Comparative Epigenomic Analysis of Murine and Human Adipogenesis

被引:431
作者
Mikkelsen, Tarjei S. [1 ]
Xu, Zhao [1 ,2 ]
Zhang, Xiaolan [1 ]
Wang, Li [1 ]
Gimble, Jeffrey M. [3 ]
Lander, Eric S. [1 ]
Rosen, Evan D. [1 ,2 ]
机构
[1] Broad Inst, Cambridge Ctr 7, Cambridge, MA 02142 USA
[2] Beth Israel Deaconess Med Ctr, Div Endocrinol & Metab, Boston, MA 02115 USA
[3] Louisiana Univ Syst, Pennington Biomed Res Ctr, Stem Cell Biol Lab, Baton Rouge, LA 70808 USA
关键词
TRANSCRIPTION FACTOR-BINDING; GENOME-WIDE ANALYSIS; RESPONSE ELEMENT; GENE-EXPRESSION; STEM-CELLS; CHROMOSOME CONFORMATION; HISTONE MODIFICATIONS; PPAR-GAMMA; DIFFERENTIATION; ENHANCERS;
D O I
10.1016/j.cell.2010.09.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the generation and comparative analysis of genome-wide chromatin state maps, PPAR gamma and CTCF localization maps, and gene expression profiles from murine and human models of adipogenesis. The data provide high-resolution views of chromatin remodeling during cellular differentiation and allow identification of thousands of putative preadipocyte- and adipocyte-specific cis-regulatory elements based on dynamic chromatin signatures. We find that the specific locations of most such elements differ between the two models, including at orthologous loci with similar expression patterns. Based on sequence analysis and reporter assays, we show that these differences are determined, in part, by evolutionary turnover of transcription factor motifs in the genome sequences and that this turnover may be facilitated by the presence of multiple distal regulatory elements at adipogenesis-dependent loci. We also utilize the close relationship between open chromatin marks and transcription factor motifs to identify and validate PLZF and SRF as regulators of adipogenesis.
引用
收藏
页码:156 / 169
页数:14
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